Variant report

Variant	nsv1029993
Chromosome Location	chr6:166621852-166695791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:806)
CpG islands
(count:1224)
Chromatin interactive
region (count:36)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:166636589-166636882	K562	blood:	n/a	n/a
2	ATF1	chr6:166691959-166692413	K562	blood:	n/a	n/a
3	ATF1	chr6:166623702-166623752	K562	blood:	n/a	n/a
4	ATF1	chr6:166672419-166672634	K562	blood:	n/a	n/a
5	ATF2	chr6:166694436-166695017	GM12878	blood:	n/a	n/a
6	ATF2	chr6:166689210-166689857	GM12878	blood:	n/a	n/a
7	ATF2	chr6:166657792-166658291	GM12878	blood:	n/a	n/a
8	ATF2	chr6:166694503-166694953	GM12878	blood:	n/a	n/a
9	ATF2	chr6:166691482-166692468	GM12878	blood:	n/a	n/a
10	ATF2	chr6:166691608-166692403	GM12878	blood:	n/a	n/a
11	ATF3	chr6:166689182-166689449	K562	blood:	n/a	n/a
12	ATF3	chr6:166672439-166672639	K562	blood:	n/a	n/a
13	BACH1	chr6:166689363-166689383	K562	blood:	n/a	n/a
14	BACH1	chr6:166666572-166667026	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:166667354-166667663	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:166689237-166689574	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr6:166694559-166695046	GM12878	blood:	n/a	n/a
18	BATF	chr6:166671279-166671679	GM12878	blood:	n/a	chr6:166671452-166671463
19	BATF	chr6:166694596-166694978	GM12878	blood:	n/a	n/a
20	BATF	chr6:166659098-166659321	GM12878	blood:	n/a	n/a
21	BATF	chr6:166691676-166692050	GM12878	blood:	n/a	n/a
22	BATF	chr6:166671359-166671577	GM12878	blood:	n/a	chr6:166671452-166671463
23	BCL3	chr6:166688326-166688550	GM12878	blood:	n/a	n/a
24	BCL3	chr6:166691726-166692456	GM12878	blood:	n/a	n/a
25	BCL3	chr6:166694567-166695035	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:166689128-166689632	GM12878	blood:	n/a	chr6:166689622-166689631
27	BHLHE40	chr6:166642049-166642253	K562	blood:	n/a	chr6:166642103-166642124
28	BHLHE40	chr6:166665315-166665415	HepG2	liver:	n/a	chr6:166665353-166665362 chr6:166665352-166665361 chr6:166665346-166665367 chr6:166665352-166665361
29	BHLHE40	chr6:166672444-166672644	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:166672363-166672674	K562	blood:	n/a	n/a
31	BHLHE40	chr6:166657820-166658335	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:166665176-166665394	GM12878	blood:	n/a	chr6:166665353-166665362 chr6:166665352-166665361 chr6:166665346-166665367 chr6:166665352-166665361
33	BHLHE40	chr6:166689176-166689592	GM12878	blood:	n/a	chr6:166689384-166689400
34	BHLHE40	chr6:166689204-166689551	HepG2	liver:	n/a	chr6:166689384-166689400
35	BHLHE40	chr6:166673038-166673321	K562	blood:	n/a	n/a
36	BHLHE40	chr6:166689211-166689557	K562	blood:	n/a	chr6:166689384-166689400
37	BHLHE40	chr6:166642738-166642742	GM12878	blood:	n/a	n/a
38	BHLHE40	chr6:166665175-166665529	K562	blood:	n/a	chr6:166665353-166665362 chr6:166665352-166665361 chr6:166665346-166665367 chr6:166665352-166665361
39	BHLHE40	chr6:166694686-166694870	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:166691496-166692090	GM12878	blood:	n/a	n/a
41	CBX3	chr6:166672354-166672742	K562	blood:	n/a	n/a
42	CBX3	chr6:166648606-166649074	K562	blood:	n/a	n/a
43	CCNT2	chr6:166689247-166689510	K562	blood:	n/a	n/a
44	CEBPB	chr6:166682937-166683297	IMR90	lung:	n/a	n/a
45	CEBPB	chr6:166666519-166666872	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr6:166691729-166692386	HepG2	liver:	n/a	n/a
47	CEBPB	chr6:166682933-166683306	K562	blood:	n/a	n/a
48	CEBPB	chr6:166676226-166676625	HepG2	liver:	n/a	chr6:166676407-166676418 chr6:166676408-166676417
49	CEBPB	chr6:166683004-166683179	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr6:166691361-166692574	GM12878	blood:	n/a	n/a

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:166667371-166667421	GM12892	blood:	n/a
2	chr6:166673846-166673896	HCT-116	colon:	n/a
3	chr6:166667211-166667261	GM12878	blood:	n/a
4	chr6:166689361-166689411	SK-N-MC	brain:	n/a
5	chr6:166667371-166667421	GM12892	blood:	n/a
6	chr6:166673846-166673896	HCT-116	colon:	n/a
7	chr6:166667211-166667261	GM12878	blood:	n/a
8	chr6:166689361-166689411	SK-N-MC	brain:	n/a
9	chr6:166667371-166667421	NHBE	bronchial:	n/a
10	chr6:166666210-166666260	HIPEpiC	eye:	n/a
11	chr6:166667897-166667947	HepG2	liver:	n/a
12	chr6:166689319-166689369	ovcar-3	ovarian:	n/a
13	chr6:166666210-166666260	GM19239	blood:	n/a
14	chr6:166666078-166666128	MCF-7	breast:	n/a
15	chr6:166689411-166689461	AG10803	skin:	n/a
16	chr6:166663488-166663538	HRE	kidney:	n/a
17	chr6:166667504-166667554	SAEC	small airway:	n/a
18	chr6:166689319-166689369	HEEpiC	esophagus:	n/a
19	chr6:166689361-166689411	PrEC	prostate:	n/a
20	chr6:166689319-166689369	H1-hESC	embryonic stem cell:	embryo
21	chr6:166689411-166689461	ProgFib	skin:	n/a
22	chr6:166665352-166665402	ECC-1	luminal epithelium:	n/a
23	chr6:166635593-166635643	Jurkat	blood:	n/a
24	chr6:166667282-166667332	BE2_C	brain:	n/a
25	chr6:166665352-166665402	HCF	heart:	n/a
26	chr6:166689411-166689461	H1-hESC	embryonic stem cell:	embryo
27	chr6:166663488-166663538	HNPCEpiC	eye:	n/a
28	chr6:166667371-166667421	MCF10A-Er-Src	breast:	n/a
29	chr6:166689411-166689461	RPTEC	kidney:	n/a
30	chr6:166667211-166667261	MCF10A-Er-Src	breast:	n/a
31	chr6:166667504-166667554	RPTEC	kidney:	n/a
32	chr6:166666838-166666888	ProgFib	skin:	n/a
33	chr6:166667504-166667554	NHDF-neo	bronchial:	n/a
34	chr6:166654907-166654957	MCF-7	breast:	n/a
35	chr6:166666838-166666888	PANC-1	pancreas:	n/a
36	chr6:166654907-166654957	HL-60	blood:	n/a
37	chr6:166667504-166667554	AG04450	lung:	fetal
38	chr6:166667211-166667261	GM12892	blood:	n/a
39	chr6:166667282-166667332	HCT-116	colon:	n/a
40	chr6:166666287-166666337	H1-hESC	embryonic stem cell:	embryo
41	chr6:166689411-166689461	GM12878	blood:	n/a
42	chr6:166667648-166667698	HEK293	kidney:	embryo
43	chr6:166689319-166689369	GM19239	blood:	n/a
44	chr6:166673846-166673896	GM06990	blood:	n/a
45	chr6:166663488-166663538	NHDF-neo	bronchial:	n/a
46	chr6:166635593-166635643	NT2-D1	testis:	n/a
47	chr6:166671495-166671545	HIPEpiC	eye:	n/a
48	chr6:166667504-166667554	GM19239	blood:	n/a
49	chr6:166671495-166671545	SK-N-SH	brain:	n/a
50	chr6:166667504-166667554	AG09319	gingival:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:166689019..166690684-chr6:166742246..166744543,2	K562	blood:
2	chr6:166569773..166571097-chr6:166688881..166689851,8	MCF-7	breast:
3	chr6:166657165..166659175-chr6:166659836..166662538,2	K562	blood:
4	chr6:166659048..166660620-chr6:166666870..166668556,2	K562	blood:
5	chr6:166688987..166689723-chr6:166795972..166796575,2	MCF-7	breast:
6	chr6:166570369..166571226-chr6:166688925..166689531,5	MCF-7	breast:
7	chr6:166674657..166677158-chr6:166678112..166679682,2	K562	blood:
8	chr6:166659048..166661337-chr6:166666386..166668556,3	K562	blood:
9	chr6:166688810..166689569-chr6:166813843..166814557,4	MCF-7	breast:
10	chr6:166667797..166669951-chr6:166670893..166673016,3	K562	blood:
11	chr6:166689127..166689809-chr6:166795241..166795961,2	K562	blood:
12	chr6:166680038..166683966-chr6:166687476..166689219,3	K562	blood:
13	chr6:166648341..166649202-chr6:166688886..166689387,2	MCF-7	breast:
14	chr6:166569966..166570828-chr6:166688046..166688718,2	MCF-7	breast:
15	chr6:166694014..166696449-chr6:166697060..166698919,2	K562	blood:
16	chr6:166667797..166669951-chr6:166670893..166673016,3	K562	blood:
17	chr3:64009224..64009746-chr6:166688785..166689353,2	MCF-7	breast:
18	chr6:166688402..166691841-chr6:166744320..166746641,3	K562	blood:
19	chr6:166659048..166661337-chr6:166666386..166668556,3	K562	blood:
20	chr6:166680851..166682611-chr6:166697523..166699301,2	K562	blood:
21	chr6:166687858..166689609-chr6:166751857..166754422,2	K562	blood:
22	chr6:166688791..166689846-chr6:166813636..166815059,15	K562	blood:
23	chr6:166664955..166667590-chr6:166668357..166669935,2	K562	blood:
24	chr6:166688799..166689857-chr6:166814003..166815015,5	MCF-7	breast:
25	chr1:173309355..173311002-chr6:166669420..166672417,2	MCF-7	breast:
26	chr6:166648341..166649202-chr6:166688886..166689387,2	MCF-7	breast:
27	chr6:166692609..166695514-chr6:166696167..166698560,2	K562	blood:
28	chr6:166664955..166667590-chr6:166668357..166669935,2	K562	blood:
29	chr6:166659048..166660620-chr6:166666870..166668556,2	K562	blood:
30	chr6:166653771..166654771-chr8:143762774..143763452,3	Hela-S3	cervix:
31	chr6:166653109..166655486-chr6:166658907..166661895,2	K562	blood:
32	chr6:166674657..166677158-chr6:166678112..166679682,2	K562	blood:
33	chr6:166680038..166683966-chr6:166687476..166689219,3	K562	blood:
34	chr6:166657950..166660698-chr6:166853746..166856485,2	K562	blood:
35	chr6:166689115..166689803-chr6:166851089..166851730,2	MCF-7	breast:
36	chr6:166657165..166659175-chr6:166659836..166662538,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGFR1OP-4	chr6:166650457-166650528	NONHSAT116034
2	lnc-FGFR1OP-13	chr6:166681557-166682431	l_3319_chr6:166676107-166682383_thyroid
3	lnc-FGFR1OP-13	chr6:166676108-166676625	l_3319_chr6:166676107-166682383_thyroid
4	lnc-FGFR1OP-4	chr6:166650457-166650528	ENSG00000233365
5	lnc-FGFR1OP-4	chr6:166668460-166668512	NONHSAT116034
6	lnc-FGFR1OP-4	chr6:166667905-166667993	NONHSAT116034
7	lnc-FGFR1OP-4	chr6:166656290-166657416	NONHSAT116034
8	lnc-FGFR1OP-4	chr6:166656290-166657197	ENSG00000233365
9	lnc-FGFR1OP-4	chr6:166670229-166670435	NONHSAT116034

No data

Variant related genes	Relation type
GNG5P1	TF binding region
RNU6-153P	TF binding region
ENSG00000233365	TF binding region
GNG5P1	CpG island
RNU6-153P	CpG island
ENSG00000233365	CpG island
ENSG00000060762	chromatin interactions
ENSG00000234616	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000198818	chromatin interactions
ENSG00000213536	chromatin interactions

Extended variants
information (count: 3260 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3260 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557470419	chr6:166621871-166621872	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184661207	chr6:166621915-166621916	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs386708448	chr6:166621955-166621956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs6908843	chr6:166621956-166621957	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs553886253	chr6:166621971-166621972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77168781	chr6:166621977-166621978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544438241	chr6:166621988-166621989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189593674	chr6:166622045-166622046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138517213	chr6:166622073-166622074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs112969860	chr6:166622131-166622132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140780238	chr6:166622132-166622133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566794690	chr6:166622137-166622138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs375548855	chr6:166622156-166622157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192211888	chr6:166622158-166622159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143205474	chr6:166622171-166622172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549295798	chr6:166622190-166622191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs576624290	chr6:166622303-166622304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374187358	chr6:166622366-166622367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576016281	chr6:166622392-166622393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567641282	chr6:166622400-166622401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185696232	chr6:166622412-166622413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146875253	chr6:166622455-166622456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78281570	chr6:166622503-166622504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57777795	chr6:166622525-166622526	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs145897929	chr6:166622610-166622611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373083228	chr6:166622716-166622717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557823499	chr6:166622720-166622721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572782114	chr6:166622740-166622741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375137228	chr6:166622764-166622765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555371553	chr6:166622810-166622811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190220051	chr6:166622832-166622833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs9356437	chr6:166622849-166622850	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs547927529	chr6:166622850-166622851	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs562591318	chr6:166622918-166622919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs559994419	chr6:166622928-166622929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs111554424	chr6:166622955-166622956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545207020	chr6:166622976-166622977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560614444	chr6:166622988-166622989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527753115	chr6:166623066-166623067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs372198883	chr6:166623074-166623075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs560906650	chr6:166623075-166623076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs59151797	chr6:166623086-166623087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs550445618	chr6:166623093-166623094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571787546	chr6:166623100-166623101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79523354	chr6:166623102-166623103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs551214393	chr6:166623116-166623117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149197100	chr6:166623167-166623168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181844409	chr6:166623185-166623186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555408369	chr6:166623186-166623187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148333786	chr6:166623202-166623203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:850 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166619000-166633200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:166621800-166622000	Enhancers	Dnd41	blood
3	chr6:166622000-166629400	Weak transcription	Dnd41	blood
4	chr6:166631200-166633200	Weak transcription	Dnd41	blood
5	chr6:166632000-166632400	Enhancers	HepG2	liver
6	chr6:166633000-166636400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:166633200-166633400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:166633200-166634200	Enhancers	Dnd41	blood
9	chr6:166634200-166634400	Flanking Active TSS	Dnd41	blood
10	chr6:166634200-166635000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
11	chr6:166634200-166636600	ZNF genes & repeats	Fetal Thymus	thymus
12	chr6:166634400-166634600	Enhancers	Spleen	Spleen
13	chr6:166634400-166634600	Enhancers	Dnd41	blood
14	chr6:166634400-166634800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr6:166634400-166634800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr6:166634400-166634800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:166634400-166635000	Enhancers	Primary T cells from cord blood	blood
18	chr6:166634400-166635000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr6:166634600-166634800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr6:166634600-166634800	Flanking Active TSS	Dnd41	blood
21	chr6:166634600-166635400	Weak transcription	Spleen	Spleen
22	chr6:166634800-166635200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:166634800-166636000	Enhancers	Dnd41	blood
24	chr6:166635000-166635200	Flanking Active TSS	Primary T cells from cord blood	blood
25	chr6:166635200-166635400	Enhancers	Primary T cells from cord blood	blood
26	chr6:166635400-166635600	Flanking Active TSS	Primary T cells from cord blood	blood
27	chr6:166635400-166636400	Enhancers	Spleen	Spleen
28	chr6:166635600-166637000	Weak transcription	Primary T cells from cord blood	blood
29	chr6:166636000-166636200	Active TSS	Stomach Mucosa	stomach
30	chr6:166636000-166636200	Bivalent Enhancer	K562	blood
31	chr6:166636000-166636600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:166636000-166636600	ZNF genes & repeats	Dnd41	blood
33	chr6:166636000-166637400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:166636000-166637600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr6:166636200-166636400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:166636200-166636400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr6:166636200-166636400	Flanking Active TSS	K562	blood
38	chr6:166636200-166636600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr6:166636200-166636600	Bivalent Enhancer	Stomach Mucosa	stomach
40	chr6:166636400-166636600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr6:166636400-166637200	Enhancers	K562	blood
42	chr6:166636400-166637800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
43	chr6:166636600-166636800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:166636600-166637000	Weak transcription	Dnd41	blood
45	chr6:166636600-166637600	Enhancers	Fetal Thymus	thymus
46	chr6:166637000-166637400	Enhancers	Dnd41	blood
47	chr6:166637000-166637600	Enhancers	Primary T cells from cord blood	blood
48	chr6:166637000-166637800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:166637200-166637400	Flanking Active TSS	K562	blood
50	chr6:166637400-166637600	Flanking Active TSS	Dnd41	blood

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